Medical Writer: Regulatory & Clinical Documentation Expert

Placements24; East London; On-site; ZAR 540,000 - 900,000; Full time

Benefits offered by this job

Competitive salary

Professional development

Diverse therapeutic exposure

Supportive environment

Job summary

Placements24 in Queenstown, Eastern Cape, is seeking a skilled Medical Writer to produce clear, accurate regulatory and scientific documents for pharmaceutical projects. You will translate complex clinical data into accessible reports for regulators, healthcare professionals, and patients.

You will collaborate with physicians, scientists, and statisticians, manage multiple projects, and ensure adherence to guidelines and timelines.

Qualifications

• Bachelor's or Master's degree in life sciences, healthcare, English, or related field.
• Minimum of 3 years of experience as a Medical Writer in pharmaceutical/biotech/medical device industry.
• Proficiency in medical terminology and clinical research processes.
• Exceptional writing, editing, and proofreading with meticulous attention to detail.

Responsibilities

• Author, edit, and review medical documents (clinical study reports, regulatory submissions, brochures, manuscripts).
• Ensure materials are scientifically accurate, grammatically correct, and comply with guidelines and regulations.
• Collaborate with physicians, scientists, and statisticians to gather information and ensure accuracy.
• Manage multiple writing projects with timely delivery of high-quality documents.
• Maintain understanding of company products, therapeutic areas, and guidelines.
• Contribute to development and refinement of templates and processes.

Skills

Medical writing

Regulatory understanding

Editing

Education

Bachelor's or Master's in life sciences

Job description

Placements24 in Queenstown, Eastern Cape, is seeking a skilled Medical Writer to produce clear, accurate regulatory and scientific documents for pharmaceutical projects. You will translate complex clinical data into accessible reports for regulators, healthcare professionals, and patients.

You will collaborate with physicians, scientists, and statisticians, manage multiple projects, and ensure adherence to guidelines and timelines.